Canonical Allele Identifier: CA2203530258

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799698A= , CM000678.2:g.4799698A=	GRCh38
NC_000016.9:g.4849699A= , CM000678.1:g.4849699A=	GRCh37
NC_000016.8:g.4789700A=	NCBI36
NG_032174.1:g.8253T= , LRG_455:g.8253T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.420T= MANE Select	ENSP00000322832.6:p.Ala140=
ENST00000322048.11:c.420T=	ENSP00000322832.5:p.Ala140=
ENST00000585653.1:n.552T=
ENST00000586153.1:c.165T=	ENSP00000464699.1:p.Ala55=
ENST00000586336.5:n.519T=
ENST00000586504.5:c.200T=
ENST00000587377.5:c.420T=	ENSP00000468343.1:p.Ala140=
ENST00000587711.5:c.118-1031T=	ENSP00000467459.1:n.118-1031T=
ENST00000587843.5:c.*158T=	ENSP00000465970.1:n.*158T=
ENST00000588201.5:c.*277T=	ENSP00000466529.1:n.*277T=
ENST00000589543.5:n.377T=
ENST00000591292.5:n.1749T=
ENST00000591392.5:c.348T=	ENSP00000467509.1:p.Ala116=
ENST00000592019.1:c.76+63T=
NM_024589.2:c.420T= , LRG_455t1:c.420T=	NP_078865.1:p.Ala140=
NR_046480.1:n.744T=
XM_006720947.2:c.420T=	XP_006721010.1:p.Ala140=
XM_006720948.2:c.150T=	XP_006721011.1:p.Ala50=
XM_006720947.4:c.420T=	XP_006721010.1:p.Ala140=
XM_006720948.4:c.150T=	XP_006721011.1:p.Ala50=
NM_024589.3:c.420T= MANE Select	NP_078865.1:p.Ala140=
NR_046480.2:n.427T=